K-number	K041280
Device name	HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500
Applicant	Felton International, Inc.
Product code	KZE
Device class	Class II
Decision date	Jun 24, 2004
Decision	Substantially Equivalent
Regulation	880.5430

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View the full FDA submission: accessdata.fda.gov

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HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500

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